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Biologics Technician

💼 Full-time🗓 2026-05-31 → 2026-07-31

Core

Operate biologics production processes and equipment to manufacture antibody drugs and drug substances while ensuring cGMP compliance.

Role type

Biologics Technician (GMP Manufacturing)

Builds

Biologics drug products (antibody drugs, ADCs, drug substances)

Domain

Biopharmaceuticals / Biologics Manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

GMP manufacturing operations, biologics process operation, equipment operation, cGMP documentation, visual inspection, in-process testing, material handling, waste disposal, SOP development

Preferred skills

Antibody drug manufacturing, ADC manufacturing, drug substance purification

Technologies

Biologics processing equipment, cGMP documentation systems

Responsibilities

Operate biologics processes and equipment efficiently, perform final product visual inspection, conduct in-process testing, verify material documentation, transfer materials to inventory, diagnose and resolve production equipment exceptions, dispose of hazardous waste, maintain detailed operational records, update Standard Operating Procedures

Seniority

Entry to Mid-level, hands-on IC

Rewrite
## Biologics Technician Location: Sligo, SO, Ireland Employment type: Part time Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . ## Responsibilities - Assigned to daily production operations, operating different equipment. - Efficiently operate all biologics processes minimizing material loss. - Documentation of all activities in line with cGMP requirements. - Perform final product visual inspection. - Perform product intermediary packaging, as applicable. - Perform all in process testing methods. - Material receipt from warehouse, verifying all pertinent documentation. - Transfer of final material to warehouse inventory. - Perform process tests and participate in qualification and validation activities as required. - Diagnose and resolve events or exceptions of production equipment and processes. - Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations, following the procedures and policies of the plant, division, and the corporation. - Keep detailed records, manual or electronic, of the operations carried out during the work shift. - Adhering to all relevant policies relating to Quality & Safety. - Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures. ## Requirements - 3rd level qualification in a relevant Science discipline. - 2 years experience in GMP manufacturing. ## Nice to Have - Antibody drug, ADC and drug substance purification experience. ## Benefits - Equal Opportunity Employer/Veterans/Disabled. - All your information will be kept confidential according to EEO guidelines. - AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Travel: No Pay Range: $ - Where We Work Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.
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